| Literature DB >> 20431271 |
Leyla Akin1, Selim Kurtoglu, Mustafa Kendirci, Mustafa Ali Akin, Michaela F Hartmann, Stefan A Wudy.
Abstract
We report herein the case of a premature infant who presented with failure to thrive, hyponatremia, hyperkalemia and metabolic acidosis. Initial serum hormone profiling suggested isolated hypoaldosteronism (aldosterone: 0.01 pg/ml, normal range: 50-900 pg/ml). A gas chromatography-mass spectrometry spot urinary steroid profile showed grossly elevated levels of 18-hydroxy-tetrahydro-11-dehydrocorticosterone (18-hydroxy-THA: 5,893 microg/l; normal upper limit 36 microg/l) and tetrahydroaldosterone (TH-Aldo: 5,749 microg/l; normal upper limit 36 microg/l) which are aldosterone precursor metabolite and aldosterone metabolite, respectively. Thus, aldosterone synthase deficiency was excluded and pseudohypoaldosteronism (PHA) was suggested. A repeated test after dilution of the serum revealed a very high level of aldosterone (6,490 pg/ml), confirming the diagnosis of PHA in this case. Copyright 2010 S. Karger AG, Basel.Entities:
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Year: 2010 PMID: 20431271 DOI: 10.1159/000281404
Source DB: PubMed Journal: Horm Res Paediatr ISSN: 1663-2818 Impact factor: 2.852